Canonical Allele Identifier: PA2826565145
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376626
ClinVar RCV Id: RCV000417803 RCV000417874 RCV000423644 RCV000425237 RCV000426379 RCV000430828 RCV000428580 RCV000431096 RCV000433855 RCV000436180 RCV000434893 RCV000435981 RCV000440656 RCV000441816 RCV000442199 RCV000444903 RCV000468362 RCV000562533 RCV001253548 RCV004017609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Lys93Glu
CA002647
NM_001276760.3:c.277A>G